A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890396



Internal ID167762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154671633..154678813hg38UCSC Ensembl
chr1:154644109..154651289hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg387181
hg197181
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890396
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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